6533b828fe1ef96bd1288484

RESEARCH PRODUCT

Zirconocene-Based Methods for the Preparation of BN-Indenes : Application to the Synthesis of 1,5-Dibora-4a,8a-diaza-1,2,3,5,6,7-hexaaryl-4,8-dimethyl-s-indacenes

J. Mikko RautiainenEvan A. PatrickWarren E. PiersHeikki M. TuononenDenis M. SpasyukMatthew M. Morgan

subject

chemistry.chemical_classification010405 organic chemistryLigandOrganic ChemistryHalidechemistry.chemical_elementAromaticity010402 general chemistry01 natural sciencesChloride0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundHydrocarbonchemistryBN-indenesmedicineOrganic chemistrySurface modificationzirconocene-based methodsPhysical and Theoretical ChemistryBoronta116Derivative (chemistry)medicine.drug

description

A method for the preparation of 3-bora-9aza-indene heterocycles based on zirconocene mediated functionalization of the ortho-CH bonds of pyridines has been developed and used to make two such compounds. Unlike other methods, the boron center in these heterocycles remains functionalized with a chloride ligand and so the compounds can be further elaborated through halide abstraction and reduction. The utility of the method was further demonstrated by applying it towards the preparation of 1,5- dibora-4a,8a-diaza BN analogues of the intriguing hydrocarbon s-indacene starting from 2,5-dimethylpyrazine. Gram quantities of one such compound was prepared and fully characterized, and both experimental and computational data is presented to compare its properties to those of the parent hydrocarbon s-indacene. These data indicate that the BN substituted derivative exhibits lowered aromaticity in relation to the hydrocarbon. peerReviewed

http://urn.fi/URN:NBN:fi:jyu-201707313376